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Photoswitchable fatty acids enable optical control of TRPV1.
scientific article published on 22 May 2015
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4455067
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25997690%20AND%20SRC:MED&resulttype=core&format=json
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8 March 2020
title
Photoswitchable fatty acids enable optical control of TRPV1
(English)
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4455067
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8 March 2020
main subject
fatty acid
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author
Gary Lewin
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5
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4455067
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8 March 2020
Rabih Moshourab
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3
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4455067
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8 March 2020
Martin Sumser
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4
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8 March 2020
Dirk Trauner
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6
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8 March 2020
author name string
James Allen Frank
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1
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4455067
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8 March 2020
Mirko Moroni
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2
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8 March 2020
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English
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22 May 2015
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8 March 2020
published in
Nature Communications
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8 March 2020
volume
6
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8 March 2020
page(s)
7118
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4455067
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8 March 2020
copyright license
Creative Commons Attribution 4.0 International
start time
22 May 2015
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exact match
https://scigraph.springernature.com/pub.10.1038/ncomms8118
0 references
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GABA blocks pathological but not acute TRPV1 pain signals
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Caged lipids as tools for investigating cellular signaling.
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29 May 2018
TRPV1 structures in distinct conformations reveal activation mechanisms
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Stomatin-domain protein interactions with acid-sensing ion channels modulate nociceptor mechanosensitivity
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29 May 2018
Optical control of TRPV1 channels
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4455067
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29 May 2018
Light at the end of the channel: optical manipulation of intrinsic neuronal excitability with chemical photoswitches
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Rapid optical control of nociception with an ion-channel photoswitch
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Restriction of transient receptor potential vanilloid-1 to the peptidergic subset of primary afferent neurons follows its developmental downregulation in nonpeptidergic neurons
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Trpv1 reporter mice reveal highly restricted brain distribution and functional expression in arteriolar smooth muscle cells
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Pungency of TRPV1 agonists is directly correlated with kinetics of receptor activation and lipophilicity
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Body-temperature maintenance as the predominant function of the vanilloid receptor TRPV1
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Inflammatory pain: the cellular basis of heat hyperalgesia.
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Inhibition of nociceptors by TRPV1-mediated entry of impermeant sodium channel blockers
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The vanilloid receptor TRPV1: 10 years from channel cloning to antagonist proof-of-concept
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Spider toxins activate the capsaicin receptor to produce inflammatory pain.
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29 May 2018
Jellyfish and other cnidarian envenomations cause pain by affecting TRPV1 channels
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Sensitization of TRPV1 by EP1 and IP reveals peripheral nociceptive mechanism of prostaglandins
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Homo- and heteromeric assembly of TRPV channel subunits.
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Anandamide and vanilloid TRPV1 receptors
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Vanilloid receptor TRPV1 is not activated by vanilloids applied intracellularly
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1 reference
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NE-19550: a novel, orally active anti-inflammatory analgesic
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Structural model reveals key interactions in the assembly of the pregnane X receptor/corepressor complex
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Crossref
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https://api.crossref.org/works/10.1038%2FNCOMMS8118
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Identifiers
DOI
10.1038/NCOMMS8118
1 reference
stated in
Europe PubMed Central
PMC publication ID
4455067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25997690%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
ADS bibcode
2015NatCo...6.7118F
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PMC publication ID
4455067
1 reference
stated in
Europe PubMed Central
PMC publication ID
4455067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25997690%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 March 2020
PubMed publication ID
25997690
1 reference
stated in
Europe PubMed Central
PMC publication ID
4455067
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25997690%20AND%20SRC:MED&resulttype=core&format=json
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8 March 2020
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